Par-1b is required for morphogenesis and differentiation of myoepithelial cells during salivary gland development.

IF 1.6 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Organogenesis Pub Date : 2016-10-01 Epub Date: 2016-11-14 DOI:10.1080/15476278.2016.1252887
Elise M Gervais, Sharon J Sequeira, Weihao Wang, Stanley Abraham, Janice H Kim, Daniel Leonard, Kara A DeSantis, Melinda Larsen
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引用次数: 0

Abstract

The salivary epithelium initiates as a solid mass of epithelial cells that are organized into a primary bud that undergoes morphogenesis and differentiation to yield bilayered acini consisting of interior secretory acinar cells that are surrounded by contractile myoepithelial cells in mature salivary glands. How the primary bud transitions into acini has not been previously documented. We document here that the outer epithelial cells subsequently undergo a vertical compression as they express smooth muscle α-actin and differentiate into myoepithelial cells. The outermost layer of polarized epithelial cells assemble and organize the basal deposition of basement membrane, which requires basal positioning of the polarity protein, Par-1b. Whether Par-1b is required for the vertical compression and differentiation of the myoepithelial cells is unknown. Following manipulation of Par-1b in salivary gland organ explants, Par-1b-inhibited explants showed both a reduced vertical compression of differentiating myoepithelial cells and reduced levels of smooth muscle α-actin. Rac1 knockdown and inhibition of Rac GTPase function also inhibited branching morphogenesis. Since Rac regulates cellular morphology, we investigated a contribution for Rac in myoepithelial cell differentiation. Inhibition of Rac GTPase activity showed a similar reduction in vertical compression and smooth muscle α-actin levels while decreasing the levels of Par-1b protein and altering its basal localization in the outer cells. Inhibition of ROCK, which is required for basal positioning of Par-1b, resulted in mislocalization of Par-1b and loss of vertical cellular compression, but did not significantly alter levels of smooth muscle α-actin in these cells. Overexpression of Par-1b in the presence of Rac inhibition restored basement membrane protein levels and localization. Our results indicate that the basal localization of Par-1b in the outer epithelial cells is required for myoepithelial cell compression, and Par-1b is required for myoepithelial differentiation, regardless of its localization.

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唾液腺发育过程中,肌上皮细胞的形态发生和分化需要 Par-1b。
唾液腺上皮细胞最初是由固态上皮细胞组成的,这些上皮细胞被组织成一个原生芽,原生芽经过形态发生和分化后,形成由内部分泌性尖头细胞组成的双层尖头,在成熟的唾液腺中,尖头被收缩性肌上皮细胞包围。初生芽是如何过渡到acini的,以前还没有记录。我们在此发现,外层上皮细胞在表达平滑肌α-肌动蛋白并分化成肌上皮细胞后,会发生垂直压缩。最外层的极化上皮细胞组装并组织基底膜的基底沉积,这需要极性蛋白 Par-1b 的基底定位。肌上皮细胞的垂直压缩和分化是否需要 Par-1b 尚不清楚。对唾液腺器官外植体中的 Par-1b 进行处理后,Par-1b 抑制的外植体显示分化的肌上皮细胞垂直压缩减少,平滑肌 α-肌动蛋白水平降低。敲除 Rac1 和抑制 Rac GTPase 的功能也抑制了分支的形态发生。由于Rac调节细胞形态,我们研究了Rac在肌上皮细胞分化中的作用。抑制 Rac GTPase 的活性同样会降低垂直压缩和平滑肌 α-肌动蛋白的水平,同时降低 Par-1b 蛋白的水平并改变其在外层细胞中的基底定位。Par-1b的基底定位需要ROCK,抑制ROCK会导致Par-1b的错误定位和细胞垂直压缩的丧失,但不会显著改变这些细胞中平滑肌α-肌动蛋白的水平。在抑制 Rac 的情况下,过表达 Par-1b 可恢复基底膜蛋白水平和定位。我们的研究结果表明,Par-1b在外上皮细胞中的基底定位是肌上皮细胞压缩所必需的,而无论其定位如何,Par-1b都是肌上皮细胞分化所必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Organogenesis
Organogenesis BIOCHEMISTRY & MOLECULAR BIOLOGY-DEVELOPMENTAL BIOLOGY
CiteScore
4.10
自引率
4.30%
发文量
6
审稿时长
>12 weeks
期刊介绍: Organogenesis is a peer-reviewed journal, available in print and online, that publishes significant advances on all aspects of organ development. The journal covers organogenesis in all multi-cellular organisms and also includes research into tissue engineering, artificial organs and organ substitutes. The overriding criteria for publication in Organogenesis are originality, scientific merit and general interest. The audience of the journal consists primarily of researchers and advanced students of anatomy, developmental biology and tissue engineering. The emphasis of the journal is on experimental papers (full-length and brief communications), but it will also publish reviews, hypotheses and commentaries. The Editors encourage the submission of addenda, which are essentially auto-commentaries on significant research recently published elsewhere with additional insights, new interpretations or speculations on a relevant topic. If you have interesting data or an original hypothesis about organ development or artificial organs, please send a pre-submission inquiry to the Editor-in-Chief. You will normally receive a reply within days. All manuscripts will be subjected to peer review, and accepted manuscripts will be posted to the electronic site of the journal immediately and will appear in print at the earliest opportunity thereafter.
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